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Conformation of 1,3,5-tri-p-tolylmethyl-1,3,5-triazacyclohexane

✍ Scribed by Bouchemma, A. ;McCabe, P. H. ;Sim, G. A.

Book ID: 114506868
Publisher: International Union of Crystallography
Year: 1990
Tongue: English
Weight: 492 KB
Volume: 46
Category: Article
ISSN: 0108-2701
DOI: 10.1107/s0108270189009364

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The title compound, C 21 H 18 F 3 N 3 O 6 S 3 , has a chair conformation that is similar to the majority of the 1,3,5-triazacyclohexane rings reported in the literature. It is the product of a condensation reaction between ¯uorobenzenesulfonamide and formaldehyde, and its empirical and structural fo

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## Abstract Relatively stable equimolar adducts of 1,3,5‐trinitro‐1,3,5‐triazacyclohexane were prepared with 2,6‐lutidine‐N‐oxide, 4‐hydroxy‐1‐butanesulfonic acid δ‐sultone (1,4‐butane sultone), and 2,2,6,6‐tetramethyl‐4‐piperidone‐1‐oxyl. Only the last adduct is selective for RDX; the others also